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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H24N5O15P3
Molecular Weight 715.3931
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3'-O-(4-BENZOYL)BENZOYLADENOSINE 5'-TRIPHOSPHATE

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](OC(=O)C4=CC=C(C=C4)C(=O)C5=CC=CC=C5)[C@H]3O

InChI

InChIKey=AWJJLYZBWRIBCZ-UGTJMOTHSA-N
InChI=1S/C24H24N5O15P3/c25-21-17-22(27-11-26-21)29(12-28-17)23-19(31)20(16(41-23)10-40-46(36,37)44-47(38,39)43-45(33,34)35)42-24(32)15-8-6-14(7-9-15)18(30)13-4-2-1-3-5-13/h1-9,11-12,16,19-20,23,31H,10H2,(H,36,37)(H,38,39)(H2,25,26,27)(H2,33,34,35)/t16-,19-,20-,23-/m1/s1

HIDE SMILES / InChI

Molecular Formula C24H24N5O15P3
Molecular Weight 715.3931
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
The azetidine derivative, KHG26792 protects against ATP-induced activation of NFAT and MAPK pathways through P2X7 receptor in microglia.
2015-12
Purinergic P2X7 receptors mediate cell death in mouse cerebellar astrocytes in culture.
2013-12
P2X7 receptors at adult neural progenitor cells of the mouse subventricular zone.
2013-10
Microglial zinc uptake via zinc transporters induces ATP release and the activation of microglia.
2011-12
Expression and functional characterization of P2X receptors in mouse alveolar macrophages.
2011-09
Characterization of protoberberine analogs employed as novel human P2X7 receptor antagonists.
2011-04-15
Pharmacological characterization of pannexin-1 currents expressed in mammalian cells.
2009-02
P2X(7) receptor blockade prevents ATP excitotoxicity in oligodendrocytes and ameliorates experimental autoimmune encephalomyelitis.
2007-08-29
Stimulation of P2X7 receptors elevates Ca2+ and kills retinal ganglion cells.
2005-06
Regulation of phospholipase D by P2X7 receptors in submandibular ductal cells.
2003-10
Pharmacological characterization of the human P2Y11 receptor.
1999-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:07:07 GMT 2025
Edited
by admin
on Mon Mar 31 19:07:07 GMT 2025
Record UNII
4P5DXU1F8Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3'-O-(4-BENZOYL)BENZOYLADENOSINE 5'-TRIPHOSPHATE
Common Name English
3'-O-(4-BENZOYL)BENZOYL ATP
Preferred Name English
ADENOSINE 5'-(TETRAHYDROGEN TRIPHOSPHATE), 3'-(4-BENZOYLBENZOATE)
Systematic Name English
Code System Code Type Description
FDA UNII
4P5DXU1F8Q
Created by admin on Mon Mar 31 19:07:07 GMT 2025 , Edited by admin on Mon Mar 31 19:07:07 GMT 2025
PRIMARY
CAS
81790-82-1
Created by admin on Mon Mar 31 19:07:07 GMT 2025 , Edited by admin on Mon Mar 31 19:07:07 GMT 2025
PRIMARY
PUBCHEM
115205
Created by admin on Mon Mar 31 19:07:07 GMT 2025 , Edited by admin on Mon Mar 31 19:07:07 GMT 2025
PRIMARY
MESH
C033901
Created by admin on Mon Mar 31 19:07:07 GMT 2025 , Edited by admin on Mon Mar 31 19:07:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID001002227
Created by admin on Mon Mar 31 19:07:07 GMT 2025 , Edited by admin on Mon Mar 31 19:07:07 GMT 2025
PRIMARY